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2. [Structure of the globin genes in persons with anomalous hemoglobins]. Kavsan VM Tsitol Genet; 1982; 16(2):62-72. PubMed ID: 6179278 [No Abstract] [Full Text] [Related]
3. Genetics of haemoglobin. Barkhan P Guys Hosp Rep; 1967; 116(3):307-22. PubMed ID: 4872865 [No Abstract] [Full Text] [Related]
4. [Genetics and molecular bases of hemoglobinopathies]. Predescu C Stud Cercet Med Interna; 1969; 10(4):313-25. PubMed ID: 5370596 [No Abstract] [Full Text] [Related]
7. [Genetics and pathology. II. Study of diseases at the molecular level]. Lisker R Gac Med Mex; 1967 Dec; 97(12):1577-82. PubMed ID: 5611799 [No Abstract] [Full Text] [Related]
12. Oxygen transport in hemoglobin Köln. Effect of increased oxygen affinity in absence of compensatory erythrocytosis. Woodson RD; Heywood JD; Lenfant C Arch Intern Med; 1974 Oct; 134(4):711-5. PubMed ID: 4414970 [No Abstract] [Full Text] [Related]
13. [Classification and physiopathologic and genetic mechanisms of hemoglobinopathies]. Orsini A; Orsini-Roubin J Ann Pediatr (Paris); 1985 Nov; 32(9):755-65. PubMed ID: 4091447 [No Abstract] [Full Text] [Related]
14. A new Spanish family with Hb Louisville. Villegas A; Malcorra JJ; Balda I; Calero F; Porres A; Alvarez-Sala JL; Espinós D Am J Med Genet; 1989 Jan; 32(1):9-14. PubMed ID: 2705488 [TBL] [Abstract][Full Text] [Related]
15. How we diagnose and manage altered oxygen affinity hemoglobin variants. Yudin J; Verhovsek M Am J Hematol; 2019 May; 94(5):597-603. PubMed ID: 30690774 [TBL] [Abstract][Full Text] [Related]
16. Unstable hemoglobinemia, Hb Buenos Aires, Bryn Mawr, followed up for eighteen years. Ando C; Moriyama K; Nakashima Y; Ohmiya A; Yoshikuni H; Moriuchi H; Tsuji Y; Ohba Y; Hattori Y; Kamitamari A Fukuoka Igaku Zasshi; 2004 Nov; 95(11):297-304. PubMed ID: 15717496 [TBL] [Abstract][Full Text] [Related]
17. [Comparative study of the primary structure of amphibian hemoglobins. Relation between structure and function. II. Abnormal human hemoglobins]. Ann Ist Super Sanita; 1968; 4(1):111-25. PubMed ID: 5734611 [No Abstract] [Full Text] [Related]
18. Secondary and tertiary structure aberration of alpha globin chain in haemoglobin Q-India disorder. Wiwanitkit V Indian J Pathol Microbiol; 2006 Oct; 49(4):491-4. PubMed ID: 17183835 [TBL] [Abstract][Full Text] [Related]
19. Sequences of G gamma, A gamma, and beta genes of the Greek (A gamma) HPFH mutant: evidence for a distal CCAAT box mutation in the A gamma gene. Gelinas R; Yagi M; Endlich B; Lotshaw C; Kazazian HH; Stamatoyannopoulos G Prog Clin Biol Res; 1985; 191():125-39. PubMed ID: 2413469 [TBL] [Abstract][Full Text] [Related]
20. Molecular analysis of Hb Q-H disease and Hb Q-Hb E in a Singaporean family. Tan J; Tay JS; Wong YC; Kham SK; Bte Abd Aziz N; Teo SH; Wong HB Southeast Asian J Trop Med Public Health; 1995; 26 Suppl 1():252-6. PubMed ID: 8629117 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]